Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
6042275 | Pediatric Neurology | 2014 | 22 Pages |
Abstract
We identified the molecular cause underlying congenital myasthenic syndrome in two patients. The marked phenotypic variation suggests that other factors including modifier genes may affect the severity of this disease.
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Authors
Hussein N. MD, Reham M. MSc, Imad Y. MD, Hayat S. BSc, Lihadh MD, Bassam R. PhD,